Yessine Amri

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 19 publications

IL-10 promoter polymorphisms (-1082G > A,-819C > Tand - 592 C > A) and pediatric asthma susceptibility in a Mauritanian population.

IL-10 promoter polymorphisms (-1082G > A,-819C > Tand - 592 C > A) and pediatric asthma susceptibility in a Mauritanian population.

Journal: The Journal of asthma : official journal of the Association for the Care of Asthma

Published: July 06, 2026

Discrepancies in Sigma Metrics Driven by Total Allowable Error Variability: Implications for QC Strategy and Laboratory Efficiency.

Discrepancies in Sigma Metrics Driven by Total Allowable Error Variability: Implications for QC Strategy and Laboratory Efficiency.

Journal: The journal of applied laboratory medicine

Published: August 25, 2025

Vitamin D deficiency in sickle cell disease: a neglected comorbidity in Tunisia.

Vitamin D deficiency in sickle cell disease: a neglected comorbidity in Tunisia.

Journal: Annals of hematology

Published: August 15, 2025

Challenges in Serum Albumin Measurements: A Comparative Study of the Bromocresol Green and the Capillary Zone Electrophoretic Method.

Challenges in Serum Albumin Measurements: A Comparative Study of the Bromocresol Green and the Capillary Zone Electrophoretic Method.

Journal: The protein journal

Published: July 17, 2025

Genetic variations in the IDUA gene in Tunisian MPS I families: Identification of a novel microdeletion disrupting substrate binding and structural insights.

Genetic variations in the IDUA gene in Tunisian MPS I families: Identification of a novel microdeletion disrupting substrate binding and structural insights.

Journal: Molecular genetics and metabolism reports

Published: October 15, 2024

Vitamin D status and VDR gene polymorphisms in patients with growth hormone deficiency: A case control Tunisian study.

Vitamin D status and VDR gene polymorphisms in patients with growth hormone deficiency: A case control Tunisian study.

Journal: Heliyon

Published: July 16, 2024

Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Insights from Ophthalmologic and Molecular Investigations in Tunisia.

Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Insights from Ophthalmologic and Molecular Investigations in Tunisia.

Journal: BMC genomics

Published: April 07, 2024

Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa.

Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa.

Journal: BMC genomics

Published: November 09, 2023

Congenital analbuminemia associated with compound heterozygous novel nucleotide variations in a young adult with coronary thrombosis.

Congenital analbuminemia associated with compound heterozygous novel nucleotide variations in a young adult with coronary thrombosis.

Journal: Annales de biologie clinique

Published: May 15, 2023

Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b.

Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b.

Journal: Diabetology & metabolic syndrome

Published: December 23, 2022

Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.

Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.

Journal: Molecular genetics & genomic medicine

Published: July 22, 2022

Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.

Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.

Journal: BMC medical genomics

Published: December 16, 2021

Showing 1-12 of 19

Last Updated: 09/26/2026